The complexity of multiple rare dental anomalies in a single mouth: microcephalic osteodysplastic primordial dwarfism type II
Microcephalic osteodysplastic primordial dwarfism type II (MOPD-II) is a rare autosomal recessive disorder caused by variants in PCNT . It is characterised by severe prenatal and postnatal growth restriction, microcephaly, skeletal anomalies, and distinctive orodental features. Fewer than 150 cases have been...